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Human Disease and Mouse Model Detail
Human Disease Neuropathy, Hereditary Sensory and Autonomic, Type IIA; HSAN2A
OMIM ID: 201300
Human Phenotype Ontology associations
Synonyms Acroosteolysis, Giaccai Type; Acroosteolysis, Neurogenic; Hsan IIA; Hsn IIA; Morvan Disease; Neuropathy, Congenital Sensory; Neuropathy, Hereditary Sensory and Autonomic; Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive; Neuropathy, Hereditary Sensory, Type IIA; HSN2A; Neuropathy, Progressive Sensory, of Children
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     FAM134B* Fam134b   HomoloGene and HGNC
KIF1A* Kif1a   HomoloGene and HGNC
SCN9A* Scn9a   HomoloGene and HGNC
WNK1* Wnk1   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory